ArticleScientific reports2025
Correlation between ADGRV1 expression and clinical pathological and prognostic features in breast cancer.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Integrative multi-omics analysis identifies SMIM24 as a favorable prognostic biomarker in clear cell renal cell carcinoma.Functional & integrative genomics · 2026Article
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12 authors.
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Abstract
Breast cancer, a leading global health threat with rising incidence, demands precision medicine guided by molecular subtyping. ADGRV1, an adhesion G protein-coupled receptor gene implicated in tumorigenesis but unexplored in breast cancer, was investigated using TCGA data (1,231 cases) and a local cohort (408 cases). While ADGRV1 showed no differential expression between tumors and normal tissues (P = 0.210), it was significantly downregulated in basal-like subtypes (P < 0.001). The association between high ADGRV1 expression and poor prognosis remains significant in the overall cohort as well as within individual molecular subtype. Functional enrichment analyses linked ADGRV1 to ribosome suppression, ECM remodeling (positive ECM-receptor interaction), and immunosuppression (negative immune pathway regulation), suggesting its role in tumor metastasis. Drug sensitivity assays demonstrated ADGRV1-high tumors confer resistance to lapatinib, gemcitabine, and 5-fluorouracil, particularly in LumB subtypes. Mechanistically, copy number variations and promoter methylation (Pearson r =-0.45, P < 0.001) regulated ADGRV1 expression, with basal-like tumors showing hypermethylation-associated suppression. These findings position ADGRV1 as a prognostic biomarker and potential therapeutic target, highlighting its dual role in tumor microenvironment modulation and drug resistance.
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